Status:
UNKNOWN
Usefulness of a Prothetic Absorbable Mesh in Incisional Hernia Prevention After Midline Laparotomy
Lead Sponsor:
Hospital Universitari Vall d'Hebron Research Institute
Conditions:
Incisional Hernia
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
Background: Development of an incisional hernia is one of the most frequent complications of midline laparotomies requiring reoperation. This paper presents the rationale, design, and study protocol f...
Eligibility Criteria
Inclusion
- Adults aged 18 years or older,
- Signed informed consent,
- Patients undergoing elective or urgent open abdominal surgical procedures regardless of benign or malignant disease.
Exclusion
- Presence of primary or recurrent incisional hernia
- Expected survival \< 12 months.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2015
Estimated Enrollment :
488 Patients enrolled
Trial Details
Trial ID
NCT02208557
Start Date
July 1 2014
End Date
July 1 2015
Last Update
August 5 2014
Active Locations (6)
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1
Hospital del Mar, Parc de Salut Mar
Barcelona, Barcelona, Spain, 08003
2
Hospital Universitari Vall d'Hebron
Barcelona, Barcelona, Spain, 08035
3
Hospital de Igualada
Igualada, Barcelona, Spain, 08700
4
Hospital Parc Taulí
Sabadell, Barcelona, Spain, 08208